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CS-W001157 4
Total: USD 88.00

3-Bromoquinoline-8-carboxylic acid

  • CAS No. 1315366-78-9

  • Cat. No. CS-0139562
  • Molecule weight252.06
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

3-Bromoquinoline-8-carboxylic acid|CS-0139562

Structure of 1315366-78-9

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General Information

  • CAS No. 1315366-78-9
  • Cat. No. CS-0139562
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₆BrNO₂
  • Molecular Weight 252.06
  • Synonym(s) 3-BROMOQUINOLINE-8-CARBOXYLICACID
  • SMILES O=C(C1=C2N=CC(Br)=CC2=CC=C1)O

Description

3-Bromoquinoline-8-carboxylic acid features a quinoline scaffold with bromine at the 3-position and a carboxylic acid group at the 8-position, enabling direct functionalization in cross-coupling and bioconjugation workflows. The electron-deficient aromatic system enhances reactivity in palladium-catalyzed transformations, while the carboxylic acid provides a handle for derivatization. This compound serves as a key intermediate in medicinal chemistry and materials synthesis.

Application

3-Bromoquinoline-8-carboxylic acid serves as a versatile building block for the synthesis of quinoline-based pharmaceutical intermediates and functional materials. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid functionality facilitates amide formation, esterification, or direct conjugation. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical choice for iterative synthetic strategies in medicinal chemistry and process development.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   50.19
  • LogP   2.6955
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   1

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